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腺病毒介导的p53对胆管癌细胞生长的抑制作用
引用本文:LU Jian-Guo,林晨,黄志强,吴金生,付明,张雪艳,梁萧,要秀,吴旻. 腺病毒介导的p53对胆管癌细胞生长的抑制作用[J]. 医学争鸣, 2000, 21(6): 764-766
作者姓名:LU Jian-Guo  林晨  黄志强  吴金生  付明  张雪艳  梁萧  要秀  吴旻
作者单位:1. 中国医学科学院,中国协和医科大学肿瘤研究所分子肿瘤学国家重点实验室,北京100021
2. 解放军总医院普外研究所,北京100853
3. 第四军医大学唐都医院普外科,陕西,西安,710038
基金项目:863高科学技术发展资助项目!( Z2 0 -0 1-0 2 )
摘    要:目的 研究P53基因对胆癌细胞的作用。方法 将重组体腺病毒P53转移到人胆管癌细胞QBC939,用RT-PCR、克隆形成实验、流式细胞仪、DNA片段化分析等方法对P53基因的表达、细胞的生长抑制及机制进行分析。结果 用Ad-LacZ进行重组体腺病毒转导致率的检测,发现当MOI为100以上时,重组体腺病毒可使90%以上的培养的人胆管癌QBC939,细胞被传导,用RT-PCR方法检测,在胆管癌QBC9

关 键 词:胆管癌 p53基因 腺病毒 基因治疗

Inhibitory effects of recombinant adenoviruses p53 transduction on human cholangiocarcinoma cell line
LU Jian-Guo,LIN Chen,HUANG Zhi-Qiang,WU Jin-Sheng,FU Ming,ZHANG Xue-Yang,LIANG Xiao,YAO Xiu,WU Ming. Inhibitory effects of recombinant adenoviruses p53 transduction on human cholangiocarcinoma cell line[J]. Negative, 2000, 21(6): 764-766
Authors:LU Jian-Guo  LIN Chen  HUANG Zhi-Qiang  WU Jin-Sheng  FU Ming  ZHANG Xue-Yang  LIANG Xiao  YAO Xiu  WU Ming
Abstract:AIM To evaluate the inhibitory effect of p53 on human cholangiocarcinoma cell line. METHODS The effects of recombinant adenoviruses p53 (Ad p53) on the growth of QBC939 cells in vitro were analyzed. RESULTS The QBC939 cell line transducted with recombinant adenoviruses LacZ ( Ad LacZ) at MOI of 100 or greater exhibited more than 90% transduction rate. p53 expression was negative in QBC939 cell but high levels of p53 expressions were observed in QBC939 cell line infected with Ad p53. The growth rates of QBC939 cells by Ad p53 at MOI of 100 inhibited reduced by 19.3%(6 day) or 24.4%(8 day) respectively (MOI of 100), compared with those of the Ad LacZ infected cells. Colony formation in these Ad p53 infected cells greatly decreased versus Ad LacZ infected cells. The Ad p53 transfected cells induced QBC939 cell apoptosis and G1 blockade, which was confirmed by the flow cytometry and DNA Ladder. CONCLUSION The suppression effects mediated by expression of the exogenous p53 on tumor cells result mainly from apoptosis and G1 blockade.
Keywords:cholangiocarcinoma  p53 gene  adenovirus  gene therapy  apoptosis
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